A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4005041



Internal ID22066672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:119278057..119284309hg38UCSC Ensembl
Outerchr8:119275864..119298868hg38UCSC Ensembl
Innerchr8:120290297..120296549hg19UCSC Ensembl
Outerchr8:120288104..120311108hg19UCSC Ensembl
Cytoband8q24.12
Allele length
AssemblyAllele length
hg3823005
hg1923005
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1154387
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4005041
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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